Draft Genomes of Methanocalculus taiwanensis P2F9704aT and Methanocalculus chunghsingensis K1F9705bT, Hydrogenotrophic Methanogens Belonging to the Family Methanocalculaceae

ABSTRACT The family Methanocalculaceae comprises hydrogen- and formate-utilizing methanogens. Here, we report two additional draft genome sequences of Methanocalculaceae, those of Methanocalculus taiwanensis P2F9704aT (equivalent to BCRC 16182T and DSM 14663T) and Methanocalculus chunghsingensis K1F9705bT (equivalent to DSM 14646T and OCM 772T), which were selected for further species delineation and comparative genomic analyses.

T he members of the genus Methanocalculus belong to the Methanocalculaceae family.
Strains P2F9704a T and K1F9705b T were isolated from an estuary of Erlin River and a marine water aquaculture fishpond near Wong-Gong, Taiwan, respectively (4,5). Both strains were grown in anaerobic MB/W medium with 100 mM sodium formate and 5 mM sodium acetate and incubated at 37°C, according to methods described previously (10)(11)(12). Genomic DNA of each strain was isolated and purified using a modification of the methods of Johnson (13) and of Jarrell et al. (14). Briefly, cells of a 500-mL culture were collected and then lysed with sodium dodecyl sulfate (1% [wt/vol]). After phenolchloroform extraction and isopropanol precipitation, the quantity and quality of the extracted DNA samples were checked by UV-visible spectrophotometry.
The genomes of both strains were sequenced at the Genomics BioSci & Tech Co., Ltd. (Taiwan) using the MiSeq platform (Illumina). For both strains, genomic DNA was sheared randomly, and a paired-end DNA library of 300 bp was constructed by using the TruSeq Nano DNA HT library prep kit and TruSeq DNA with 96 CD indexes (Illumina). The constructed library was sequenced using a MiSeq reagent kit v3 (600 cycles), and 6,537,788 and 4,735,720 reads were generated for strains P2F9704a T and K1F9705b T , respectively. All generated reads were quality trimmed to obtain high-quality reads using Trimmomatic v0.36 (15). For the genome de novo assembly, the genome assembler of Shovill v1.0.4 (16) was applied. The sequencing protocol generated ;425-fold and ;547-fold mean coverage for the genomes of strains P2F9704a T and K1F9705b T , respectively. Genes of the genome were identified using the Prokaryotic Genome Annotation pipeline (PGAP) of the National Center for Biotechnology Information (http://www.ncbi.nlm.nih.gov) (17). For the draft genome of strain P2F9704a T , a total of 69 contigs were obtained with an N 50 value of 72,685 bp and a total size of 2,342,634 bp with a 50.41% GC content. The genome was predicted to harbor 2,348 genes. For strain K1F9705b T , a total of 51 contigs were obtained with an N 50 value of 84,108 bp and total size of 2,134,545 bp with a 52.22% GC content. The genome was predicted to harbor 2,253 genes. No plasmid was identified in either genome using PlasmidFinder (18). Default parameters were used for all software unless otherwise specified.
Data availability. These whole-genome shotgun projects for strains P2F9704a T and K1F9705b T have been deposited in GenBank under the accession numbers VOTZ00000000 and JWHL00000000, respectively. The versions for each genome described in this paper are the respective first versions. The BioProject accession numbers for strains P2F9704a T and K1F9705b T are PRJNA559048 and PRJNA224116, respectively. The raw sequence reads for strains P2F9704a T and K1F9705b T have been deposited in the Sequence Read Archive under accession numbers SRR18085627 and SRR20645508, respectively.

ACKNOWLEDGMENTS
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